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2-trimethylsilyloxy-1-phenoxy-3-chloropropane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18036-64-1

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18036-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18036-64-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,0,3 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18036-64:
(7*1)+(6*8)+(5*0)+(4*3)+(3*6)+(2*6)+(1*4)=101
101 % 10 = 1
So 18036-64-1 is a valid CAS Registry Number.

18036-64-1Downstream Products

18036-64-1Relevant academic research and scientific papers

Cobalt(II) Chloride Catalysed Regioselective Cleavage of Oxiranes with Chlorotrimethylsilane

Iqbal, Javed,Khan, Mohd. Amin

, p. 1157 - 1158 (1988)

Oxiranes can be cleaved regioselectively with chlorotrimethylsilane in presence of cobalt(II) chloride to the corresponding O-silylated vicinal chlorohydrins in excellent yields.

Catalysis mechanisms in the reaction of chlorotrimethylsilane with 1-phenoxy-2,3-epoxypropane

Popov,Anikeev,Kostenko,Koblik

, p. 258 - 262 (2007/10/03)

The efficient catalysis with tetraethylammonium chloride and pyridine in the reaction between chlorotrimethylsilane and 1-phenoxy-2,3-epoxypropane occurs along two independent pathways: of basic and of nucleophilic character. The quantitative evaluation o

REGIOSELECTIVITY, KINETICS, AND MECHANISM OF THE ADDITION OF TRIMETHYLCHLOROSILANE TO 1-PHENOXY-2,3-EPOXYPROPANE

Popov, A. F.,Anikeev, A. V.,Kostenko, L. I.,Koblik, I. V.

, p. 413 - 417 (2007/10/02)

The reaction of trimethylchlorosilane with 1-phenoxy-2,3-epoxypropane takes place through the silylation of 1-phenoxy-3-chloro-2-propanol. The regioselectivity of the process is determined by the regioselectivity of hydrochlorination of the α-oxide, while the rate is determined by the concentration of its corresponding α-chlorohydrin.

SODIUM BROMIDE CATALYSED REGIOSELECTIVE CLEAVAGE OF OXIRANES WITH CHLOROTRIMETHYLSILANE

Iqbal, Javed,Khan, M. Amin,Ahmad, Saeed

, p. 641 - 644 (2007/10/02)

Sodium bromide efficiently catalyses the regioselective cleavage of oxiranes with chlorotrimethylsilane to the corresponding O-silyiated chlorohydrins in excellent yield.

NUCLEOPHILIC CATALYSIS IN THE INSERTION OF SILICON HALIDES INTO OXIRANES: A SYNTHESIS OF O-PROTECTED VICINAL HALOHYDRINS

Andrews, Glenn, C.,Crawford, Thomas C.,Contillo, Leonard G.

, p. 3803 - 3806 (2007/10/02)

Silicon halides in the presence of nucleophilic catalysts react with epoxides to form O-protected vicinal halohydrins with enhanched regioselectivity.

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